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scilearner

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Posts posted by scilearner

  1. inserting2.gif

     

    1. Ok in the plasmid we used the ECOR1 to create sticky ends. Now my question is when we add DNA ligase, why don't these ends stick back again. How are we able to add new DNA piece in between. Basically what I'm saying is when ECOR 1 creates sticky ends in plamids, why do they separate the plamid, don't the sticky ends stick back together.

     

    2. Also why can't DNA ligase bind the blunt ends, can't it fix the phosphodiester bond there.

     

    Thanks :)

  2. Hello everyone,

     

    RestrictionEnzymes.gif

     

    1. Restriction enzymes cut only sugar phospahte bonds right. So in the formation of sticky bonds for example in BamHl, how does the hydrogen bonds between the molecules break. When sugar phophate bonds on each strand break, does it pull on the free side dissociating the hydrogen bonds. Can these pieces stick back easily again or do they need a ligase?

     

    2. Can restriction enzymes cut single stranded DNA?

     

    3. Also how do these detect specific sequences of DNA. Do they have some complementary area that binds with the specific region.

     

    Thanks :)

  3. Hello everyone,

     

    I don't understand how depolarisation jumps when axons are myelinated. Ok myelin is an insulator so in that section no current passes through. But how does that make the current jump, when current reached myelin wouldn't it be inhibited, why does it still travel. Also what do they mean by developing current sinks at nodes of ranvier. Thanks :)

  4. Hello everyone,

     

    Ok I'm confused again (surprise). Let's say there is a semipermeable membrane and on one side there was 100 percent water. On the other side there are solutes mixed with water. Now water should move from high to low, but where is the water from 100 percent side going to move into. There are no gaps on other side, other side is full of water mixed with solutes. So why does it diffuse. Thanks :)

  5. Hello everyone,

     

    I know nerve fibres inside brain are not covered by perineurium etc like Peripheral nervous system. Are they still covered with connective tissue, support cells, myelin etc. I mean inside the brain , a collection of nerve fibres, how are they held together with no connective tissue. I don't have much knowledge about brain. Thanks :)

  6. Now I'm confused. Ok let's say there is a container with oxygen (Pa=100mmHg) and carbon dioxide (p=20mmHg) . Now total pressure is 120 mmHg. So if I remove carbon dioxide, the total pressure in the chamber becomes 100 mmHg. Is that right?

     

    Ok but inside the lung there is oxygen and carbon dioxide. If I breathe fast and remove carbon dioxide, the partial pressure of oxygen increases? Why is that? When carbon dioxide is rapidly removed, does more oxygen from atmosphere enter the lung. Is that the reason. Please answer both questions. Thanks :)

  7. Hello everyone,

     

    This is what I'm thinking. Tell me if this is wrong

     

    Blood cerebrospinal fluid barrier: Blood goes through ependymal cells, which filter it, and create CSF that circulates in brain.

    Blood brain barrier: This create CSF is further protected from incoming blood vessels, by this barrier allowing only some to diffuse.

     

    Also what is tela choroidea, I know it is two layered fold of pia matter but how is helping to form chorodal plexus. Do blood vessel come from it?

     

    Thanks :smile:

  8. Hello everyone,

     

    I'm confused with partial pressure of a gas.

     

    Wiki: In a mixture of ideal gases, each gas has a partial pressure which is the pressure which the gas would have if it alone occupied the volume.

     

    Now in a container if I have oxygen and carbon dioxide. If I remove carbon dioxide, shouldn't the oxygen occupy more space and its pressure decrease. So how can you call partial pressure of a gas pressure which the gas would have if it alone occupied the volume. Thanks :)

  9. Hello everyone,

     

    There was a simple question given, where there was a bee sting on a guy and the question asked was what is the antibody involved. The answer is IgE. Now my question is when there is bee sting for the first time, why do we called it an allergic reaction. I mean for an allergy to occur don't we have to be exposed to the antigen second time, so IgE attached to Mast cells will release histamine 2nd time. Also why aren't other antibodies like IgA ect not involed in a bee sting. Thanks :)

  10. Hello everyone,

     

    I'm slightly confused here. After ovulation, progesterone increases markedly. Now progesterone is also used as a contraceptive for creating a hostile environment for fertilisation and not allowing sperm to enter. So after ovulation how does fertilisation occur normally, if progesterone increases right after that. I see that it takes like 5 days for progesterone to peak. So does fertilisation have to occur before progesterone increases a lot. Also after fertilisation, doesn't the effects of progesterone cause any problems to the fertilized egg. Thanks :)

  11. Hello everyone,

     

    I searched the net but I don't understand the difference.

     

    BLO0D FLOW ---------------------------------->

    0% ........................................… saturation

    0% ........................................… saturation

    WATER FLOW <-------------------------------

     

    Countercurrent

     

    BLO0D FLOW ---------------------------------->

    0% ........................................… saturation

    100%..................................… saturation

    WATER FLOW --------------------------------->

     

    Concurrent

     

    I understand how equilibrium would be reached in concurrent but I don't understand how counter current maintains a concentration gradient. Please explain in simple language. Also if you can explain the above diagrams, I got it from net I don't understand them much. Thanks :)

  12. Hello everyone,

     

    What I just read is for type 1 diabetes mellitus, it requires an environmental factor (eg virus) and genetic determinant that allows the B cells to be detected as non self. Now I'm not very familiar with autoimmune diseases. My question is why does a virus have to come and trigger the autoimmune destruction of B cells. If B cells are alreadly genetically non self, shouldn't the body start attacking them without a stimulus? Thank you :)

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